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Items: 1 to 20 of 172

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    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv7097022copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-138,861,289 , GRCh38.p12 chr5: 137,622,098-139,481,704 CDC25C, SLC23A1, 55 more genes
    nsv7096751copy number variation1nstd102humanUncertain significance GRCh37 chr5: 136,957,787-140,078,137 , GRCh38.p12 chr5: 137,622,098-140,698,552 CDC25C, LOC100128966, 94 more genes
    nsv7051532inversion1nstd229human GRCh38 chr5: 138,571,961-138,578,105 , GRCh37.p13 chr5: 137,907,650-137,913,794 LOC105379193, HSPA9
    nsv6791143copy number variation1nstd229human GRCh38 chr5: 138,553,772-138,553,855 , GRCh37.p13 chr5: 137,889,461-137,889,544 HSPA9
    nsv6788339copy number variation1nstd229human GRCh38 chr5: 138,571,271-138,694,782 , GRCh37.p13 chr5: 137,906,960-138,030,471 RPL10AP10, LOC105379193, 1 more genes
    nsv6636861copy number variation1nstd102humanUncertain significance GRCh37 chr5: 137,893,096-138,868,605 , GRCh38.p12 chr5: 138,557,407-139,489,020 HSPA9, ECSCR, 27 more genes
    nsv6405600copy number variation1nstd223human GRCh38 chr5: 137,606,101-142,582,700 , GRCh37.p13 chr5: 136,941,790-141,962,265 TMCO6, PCDHB17P, 191 more genes
    nsv6298279copy number variation1nstd186human GRCh37 chr5: 137,897,507-137,898,181 , GRCh38.p12 chr5: 138,561,818-138,562,492 HSPA9
    nsv6295419copy number variation1nstd186human GRCh37 chr5: 137,891,805-137,892,140 , GRCh38.p12 chr5: 138,556,116-138,556,451 HSPA9
    nsv6244883mobile element insertion1nstd215human GRCh38 chr5: 138,567,772-138,567,772 , GRCh37.p13 chr5: 137,903,461-137,903,461 HSPA9
    nsv6135383copy number variation1nstd213human GRCh37 chr5: 137,050,000-138,100,001 , GRCh38.p12 chr5: 137,714,311-138,764,312 CDC25C, CTNNA1, 32 more genes
    nsv6135205copy number variation1nstd213human GRCh37 chr5: 91,690,000-180,740,001 , GRCh38.p12 chr5: 92,354,293-181,313,000 ADRA1B, ASS1P10, 1378 more genes
    nsv6135115copy number variation1nstd213human GRCh37 chr5: 137,330,000-138,340,001 , GRCh38.p12 chr5: 137,994,311-139,004,312 HSPA9, KIF20A, 27 more genes
    nsv6004186copy number variation1nstd212human GRCh38 chr5: 138,562,355-138,562,442 , GRCh37.p13 chr5: 137,898,044-137,898,131 HSPA9
    nsv5951476insertion1nstd209human GRCh38 chr5: 138,553,611-138,553,611 , GRCh37.p13 chr5: 137,889,300-137,889,300 HSPA9
    nsv5892800copy number variation1nstd209human GRCh38 chr5: 138,553,442-138,553,588 , GRCh37.p13 chr5: 137,889,131-137,889,277 HSPA9
    nsv5721675mobile element insertion1nstd211human GRCh38 chr5: 138,571,976-138,571,976 , GRCh37.p13 chr5: 137,907,665-137,907,665 LOC105379193, HSPA9
    nsv5715335mobile element insertion1nstd211human GRCh38 chr5: 138,572,247-138,572,247 , GRCh37.p13 chr5: 137,907,936-137,907,936 HSPA9, LOC105379193
    nsv5643296insertion1nstd207human GRCh38 chr5: 138,572,247-138,572,247 , GRCh37.p13 chr5: 137,907,936-137,907,936 HSPA9, LOC105379193
    nsv5563220mobile element insertion1nstd206human GRCh38 chr5: 138,572,262-138,572,298 , GRCh37.p13 chr5: 137,907,951-137,907,987 HSPA9, LOC105379193
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